The largest database of trusted experimental protocols

5 protocols using medium molecular weight chitosan powder

1

Antibacterial Polymer Nanocomposite Synthesis

Check if the same lab product or an alternative is used in the 5 most similar protocols
WS2 powder, having an average nanoparticle size of 80 to 100 nm, was purchased from Lower Friction Company (Mississauga, ON, Canada). P(3HB-co-12 mol% HHx) powder (350,000 Da) was obtained from KANEKA Corporation, Osaka, Japan. Medium molecular weight chitosan powder was purchased from Sigma-Aldrich, St. Louis, MO, USA. Glacial acetic acid (99.8%) was obtained from Sigma-Aldrich, Petaling Jaya, Malaysia. Bacterial cultures of E. coli K1 and MRSA were grown and incubated for up to 16 h prior to antibacterial analysis. LDH kit was purchased from Roche Diagnostics, Indianapolis, IN, USA. Non-essential amino acid was purchased from Life Technologies, Carlsbad, CA, USA. In this experiment, analytical-grade reagents were used.
+ Open protocol
+ Expand
2

Chitosan Crosslinking for Biomaterials

Check if the same lab product or an alternative is used in the 5 most similar protocols
Medium molecular weight chitosan powder (~250,000 g/mol) with a DD of 75–85% was obtained from Sigma-Aldrich (St. Louis, MO, USA). A glutaraldehyde (GA) solution (25%) was purchased from SHOW (Tokyo, Japan) and used as a crosslinking agent. HCl, NaOH, CuCl∙2H2O, and KH2PO4 were purchased from Sigma-Aldrich (St. Louis, MO, USA). All chemicals were used as received without further purification.
+ Open protocol
+ Expand
3

Chitosan-Gluconic Acid Hydrogel Synthesis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Medium-molecular-weight chitosan powder was
purchased from Sigma-Aldrich. Gluconic acid δ-lactone (GDL)
and sodium tetraborate decahydrate (borax) were supplied from Sigma-Aldrich
(Italy). All solutions were prepared using deionized Milli-Q water
(resistivity 18.2 MΩ.cm).
+ Open protocol
+ Expand
4

Chitosan-Helix aspersa Scaffold Fabrication

Check if the same lab product or an alternative is used in the 5 most similar protocols
Medium-molecular-weight chitosan powder (Sigma-Aldrich), Helix aspersa mucus extract (Medical Grade, Xi’an
SR Bio-Engineering Co., Ltd.), and Helix aspersa slime
extract (Pharmaceutical Grade) (Xi’an Nate Biological Technology
Co., Ltd.) were used for scaffold fabrication. Eagle’s MEM
(Capricorn Scientific), penicillin/streptomycin, and l-glutamine
(Lonza) were used in cell culture studies. The WST-1 assay (BioVision
Inc.), Enzyline PAL Optimise ALP kit (Biomerieux, France), Human Osteocalcin
and Human Cartilage Oligomeric Matrix Protein (COMP) Sandwich-ELISA
Kits (Elabscience), and proteoglycan assay (Amsbio, AMS Biotechnology)
were used for in vitro bioactivity studies. Hematoxylin
& eosin (Mayer’s), Masson’s Trichrome (Bio-Optica,
04-010802), Alcian Blue (ScienCell 8378), Alizarin Red S Staining
kit (Abcam ab146374), Safranin O Staining kit (ScienCell 8348), type
I collagen (bs-10423R, Bioss), and type II collagen (bs-0709R, Bioss)
were used for histology staining protocols. Silver nitrate and sodium
thiosulfate (Sigma-Aldrich) were used for the biomineralization study.
+ Open protocol
+ Expand
5

Chitosan Coatings with Essential Oils

Check if the same lab product or an alternative is used in the 5 most similar protocols
Chitosan coatings were prepared according to the method of Pabast et al. [22 (link)], with some modifications. The chitosan solution (2%) was made by dissolving medium molecular weight chitosan powder (Sigma-Aldrich, St. Louis, MO, USA) in 1% acetic acid (>99.8%, Centrohem, Stara Pazova, Serbia) by stirring with a magnetic stirrer (SCILOGEX SCI280-Pro, Rocky Hill, CT, USA) for 2 h at 95 °C. After filtering the resulting solutions, 0.25 mL/g of glycerol (98+%, Fisher Scientific, Loughborough, UK) was added to the chitosan solution. Stirring was continued for 30 min at room temperature. Thereafter, a surfactant, Tween 60 (Fisher Scientific, Loughborough, UK), at a concentration of 0.1% was added and stirring was continued at 60 °C for 30 min. After cooling to room temperature, Satureja montana L. essential oil (SMEO) or nanoparticles in concentrations of 0.25%, 0.5% and 1% was added to the chitosan coating.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!